达玛小袋鼠的早期卵巢分化及暴露于双酚 A 的影响。

IF 3.7 3区 生物学 Q1 DEVELOPMENTAL BIOLOGY Reproduction Pub Date : 2024-11-01 DOI:10.1530/REP-24-0259
Mario T Peiris, Yu Chen, Geoffrey Shaw, Marilyn B Renfree
{"title":"达玛小袋鼠的早期卵巢分化及暴露于双酚 A 的影响。","authors":"Mario T Peiris, Yu Chen, Geoffrey Shaw, Marilyn B Renfree","doi":"10.1530/REP-24-0259","DOIUrl":null,"url":null,"abstract":"<p><p>Bisphenol-A (BPA), an environmental endocrine disruptor (EED), is used widely in the manufacturing of various plastics. While BPA can have detrimental effects on fertility and reproductive health, the effects of BPA on early ovarian differentiation in mammals remains unclear. Marsupials have undifferentiated gonads at birth, so this study investigated the gross morphology, protein localisation of FOXL2 and FST and the expression profile of key ovarian differentiating genes FOXL2, WNT4,FST, ESR1 and ESR2 every 2 days from the day of birth to day 10 post partum (pp) in the marsupial tammar wallaby. A second group of newborn female pouch young were treated with 50 µg/kg of BPA daily from day 0-10 pp and the morphology and gene expression were examined at day 10 pp. Ovigerous cords in tammar ovaries were first formed between days 2 to 4 pp. FOXL2 localisation became nuclear by day 4 in pre-granulosa cells. FST was initially in the cytoplasm of pre-granulosa cells at day 2 pp, but was then secreted into the extracellular matrix in ovaries by day 10 pp. FOXL2, FST, ESR1 and ESR2 mRNA were upregulated in ovaries around day 2-4 pp, indicating that ovarian differentiation in the tammar begins from day 2-4 pp. Interestingly, BPA treatment from day 0-10 pp blocked the morphological differentiation of the cortex and medulla as well as ovigerous cord formation and downregulated the expression of FST and FOXL2 at day 10 pp.</p>","PeriodicalId":21127,"journal":{"name":"Reproduction","volume":" ","pages":""},"PeriodicalIF":3.7000,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Early ovarian differentiation in the tammar wallaby and the effects of exposure to bisphenol-A.\",\"authors\":\"Mario T Peiris, Yu Chen, Geoffrey Shaw, Marilyn B Renfree\",\"doi\":\"10.1530/REP-24-0259\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Bisphenol-A (BPA), an environmental endocrine disruptor (EED), is used widely in the manufacturing of various plastics. While BPA can have detrimental effects on fertility and reproductive health, the effects of BPA on early ovarian differentiation in mammals remains unclear. Marsupials have undifferentiated gonads at birth, so this study investigated the gross morphology, protein localisation of FOXL2 and FST and the expression profile of key ovarian differentiating genes FOXL2, WNT4,FST, ESR1 and ESR2 every 2 days from the day of birth to day 10 post partum (pp) in the marsupial tammar wallaby. A second group of newborn female pouch young were treated with 50 µg/kg of BPA daily from day 0-10 pp and the morphology and gene expression were examined at day 10 pp. Ovigerous cords in tammar ovaries were first formed between days 2 to 4 pp. FOXL2 localisation became nuclear by day 4 in pre-granulosa cells. FST was initially in the cytoplasm of pre-granulosa cells at day 2 pp, but was then secreted into the extracellular matrix in ovaries by day 10 pp. FOXL2, FST, ESR1 and ESR2 mRNA were upregulated in ovaries around day 2-4 pp, indicating that ovarian differentiation in the tammar begins from day 2-4 pp. Interestingly, BPA treatment from day 0-10 pp blocked the morphological differentiation of the cortex and medulla as well as ovigerous cord formation and downregulated the expression of FST and FOXL2 at day 10 pp.</p>\",\"PeriodicalId\":21127,\"journal\":{\"name\":\"Reproduction\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":3.7000,\"publicationDate\":\"2024-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Reproduction\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1530/REP-24-0259\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"DEVELOPMENTAL BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Reproduction","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1530/REP-24-0259","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"DEVELOPMENTAL BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

双酚 A(BPA)是一种环境内分泌干扰物(EED),广泛用于制造各种塑料。虽然双酚 A 会对生育和生殖健康产生有害影响,但双酚 A 对哺乳动物早期卵巢分化的影响仍不清楚。有袋类动物刚出生时性腺尚未分化,因此本研究调查了有袋类动物塔马壁虎从出生到产后第 10 天(pp)期间每两天的总形态、FOXL2 和 FST 的蛋白定位以及关键卵巢分化基因 FOXL2、WNT4、FST、ESR1 和 ESR2 的表达谱。第二组刚出生的雌性小袋鼠在产后第 0-10 天每天接受 50 µg/kg 的双酚 A 处理,并在产后第 10 天检测其形态和基因表达。达玛熊卵巢中的排卵索在第2至第4天开始形成。在前颗粒细胞中,FOXL2的定位在第4天变成了核定位。FST 最初在第 2 天时出现在前颗粒细胞的细胞质中,但随后在第 10 天时分泌到卵巢的细胞外基质中。卵巢中的FOXL2、FST、ESR1和ESR2 mRNA在第2-4天左右上调,这表明大马的卵巢分化从第2-4天开始。有趣的是,从第0-10 pp天开始处理双酚A会阻止皮层和髓质的形态分化以及卵巢索的形成,并在第10 pp天时下调FST和FOXL2的表达。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Early ovarian differentiation in the tammar wallaby and the effects of exposure to bisphenol-A.

Bisphenol-A (BPA), an environmental endocrine disruptor (EED), is used widely in the manufacturing of various plastics. While BPA can have detrimental effects on fertility and reproductive health, the effects of BPA on early ovarian differentiation in mammals remains unclear. Marsupials have undifferentiated gonads at birth, so this study investigated the gross morphology, protein localisation of FOXL2 and FST and the expression profile of key ovarian differentiating genes FOXL2, WNT4,FST, ESR1 and ESR2 every 2 days from the day of birth to day 10 post partum (pp) in the marsupial tammar wallaby. A second group of newborn female pouch young were treated with 50 µg/kg of BPA daily from day 0-10 pp and the morphology and gene expression were examined at day 10 pp. Ovigerous cords in tammar ovaries were first formed between days 2 to 4 pp. FOXL2 localisation became nuclear by day 4 in pre-granulosa cells. FST was initially in the cytoplasm of pre-granulosa cells at day 2 pp, but was then secreted into the extracellular matrix in ovaries by day 10 pp. FOXL2, FST, ESR1 and ESR2 mRNA were upregulated in ovaries around day 2-4 pp, indicating that ovarian differentiation in the tammar begins from day 2-4 pp. Interestingly, BPA treatment from day 0-10 pp blocked the morphological differentiation of the cortex and medulla as well as ovigerous cord formation and downregulated the expression of FST and FOXL2 at day 10 pp.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Reproduction
Reproduction 生物-发育生物学
CiteScore
7.40
自引率
2.60%
发文量
199
审稿时长
4-8 weeks
期刊介绍: Reproduction is the official journal of the Society of Reproduction and Fertility (SRF). It was formed in 2001 when the Society merged its two journals, the Journal of Reproduction and Fertility and Reviews of Reproduction. Reproduction publishes original research articles and topical reviews on the subject of reproductive and developmental biology, and reproductive medicine. The journal will consider publication of high-quality meta-analyses; these should be submitted to the research papers category. The journal considers studies in humans and all animal species, and will publish clinical studies if they advance our understanding of the underlying causes and/or mechanisms of disease. Scientific excellence and broad interest to our readership are the most important criteria during the peer review process. The journal publishes articles that make a clear advance in the field, whether of mechanistic, descriptive or technical focus. Articles that substantiate new or controversial reports are welcomed if they are noteworthy and advance the field. Topics include, but are not limited to, reproductive immunology, reproductive toxicology, stem cells, environmental effects on reproductive potential and health (eg obesity), extracellular vesicles, fertility preservation and epigenetic effects on reproductive and developmental processes.
期刊最新文献
IMPACT OF REAL-LIFE ENVIRONMENTAL EXPOSURES ON REPRODUCTION: A contemporary review of machine learning to predict adverse pregnancy outcomes from pharmaceuticals, including DDIs. O-GlcNAc participates in the meiosis of aging oocytes by mediating mitochondrial function. REPRODUCTIVE HEALTH IN TRANS AND GENDER-DIVERSE PATIENTS: Trauma-informed reproductive care for transgender and nonbinary people. SON controls mouse early embryonic development by regulating RNA splicing and histone methylation. IMPACT OF REAL-LIFE ENVIRONMENTAL EXPOSURES ON REPRODUCTION: Systemic and ovarian impacts of heat stress in the porcine model.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1